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Tafluprost acid-d4
Biological Activity:Tafluprost acid-d4 is the deuterium labeled Tafluprost acid. Tafluprost acid (AFP-172), an active metabolic form of Tafluprost, is a selective prostanoid FP receptor agonist. Tafluprost acid shows a high affinity for human prostanoid FP receptor with Ki and EC50 values of 0.4 nM and 0.53 nM, respectively. Tafluprost acid has 126 times weaker binding affinity for prostanoid EP3 receptor (IC50=67 nM) than for the prostanoid FP receptor. Tafluprost acid can be used in the research of glaucoma[2][3].
Research Area:Endocrinology|Neurological Disease|Cardiovascular Disease
Targets:Drug Metabolite|Prostaglandin Receptor
Related Small Molecules:Nicotinamide N-oxide;4-Hydroxyphenylbutazone;Omidenepag isopropyl;Ampyrone;Resveratrol-3-O-sulfate sodium;DG-041;Sonidegib metabolite M48;Isonicotinic acid;8-Isoprostaglandin E2;BAY-6672;trans-Isoferulic acid;Cycloguanil hydrochloride;GSK-269984A;KMN-80;Hydroxytanshinone IIA;SC 51089;Endoxifen;p-Hydroxycinnamic acid
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